- Merck (Rahway, NJ)
- …Supplies Management , Clinical Supply Chain Management , Clinical Testing, Clinical Trial Management , Cross-Functional Team Leadership, ... spokesperson at clinical development related meetings (ie, Clinical Trial Teams) and product development related... management and clinical customer relationship management . + Technical Proficiency: familiarity with supply … more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …_Experience Qualifications:_ + 7 or More Years of related experience, including Project Management , Clinical Supply Management , and/or Pharmaceutical ... Supply Plans in close communication with CSO project Management Lead. + Responsible for the Clinical ... Planning as requested. + Responsible for updating relevant Trial Master Files (TMF) with CSO-related documents. + Supports… more
- Sanofi Group (Morristown, NJ)
- …assigned. Take part in the Sanofi Research & Development organization and join our Clinical Supply Chain Project Management (CSC-PM) department within ... **Job Title:** Clinical Supply Chain Project Leader **Location**...supplies needed to conduct any Sanofi Pharma and Vaccine clinical trial are set up, planned, ordered,… more
- Merck (Rahway, NJ)
- …Clinical Trial Operations (GCTO), Preclinical Development Sciences and Clinical Supply (PSCS), Procurement, Subject Matter Experts (SMEs), Translational ... patients with quality products? Within our Research and Development Division, the Global Clinical Supply (GCS) organization is accountable for the end-to-end … more
- Merck (Rahway, NJ)
- …Supplies Management , Clinical Supply Chain Management , Clinical Testing, Clinical Trial Management , Cross-Functional Team Leadership, ... but are not limited to:** + Participates on the Clinical Trial Team (CTT) and collaborates closely...Clinical Supply (packaging, labeling, logistics and clinical supply inventory management ) +… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …Provides medical input regarding country feasibility. Consulted on decisions related to clinical trial feasibility and contributes to the site feasibility ... of medical accountability and oversight for one or more clinical trials + Matrix management responsibilities across...achieve the Target Product Profile (TPP) + Development of clinical sections of trial -level regulatory documents (eg,… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …_Experience Qualifications_ + 7 or More Years of related experience, including Project Management , Clinical Supply Management , and/or Pharmaceutical ... management of Dose Preparation Instructions in support of clinical studies being conducted globally by Daiichi Sankyo. The...Logistics (SP&L) function with assigned tasks related to steady supply of Clinical Trial Materials… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …submission documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to ... Planning and Execution: Provides input on major milestones of trial , clinical trial plan and...trial plan and contingency planning; Analyzes and updates management on potential risks to study deliverables; Provides input… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …components of a large-scale global clinical program using strong clinical project and program management , leadership, decision-making ability, people ... Years and Counting!** Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …or oversees the cross-functional clinical development team + Supports Global Clinical Operations in clinical trial initiation, resource planning, study ... Development is responsible for the development, execution and management of several clinical programs worldwide across...Works with Clinical Supplies Group to ensure clinical drug supply plans and timely procurement… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …(eg, CRO); oncology, immunology, or complex disease Strong knowledge of Clinical trial data systems and/or EDC lab management . required - 4+ years combined ... and laboratory data expertise to promote and implement best practices across the Clinical Trial lifecycle. - Applies GCP principles to ensure all laboratory… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …data acquisition, validation, and reconciliation, study data protection, operational metrics, and clinical trial quality and risk management reporting ... data acceptance and reconciliation reports, study data protection, operational metrics, and clinical trial quality and risk management reporting… more
- Daiichi Sankyo Inc. (Somerset County, NJ)
- …disease preferred - 7 or more years of working knowledge of Clinical trial data systems and/or EDC lab management tools is a preferred Daiichi Sankyo, ... expertise to promote and implement best practices across the Clinical Trial lifecycle. Remains current with and...CFR preferred - 7 or more years' experience in clinical data management experience in a medical… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …vs retrospective analyses and collection, missing data, demographic/representativeness of samples from clinical trial and screen failures. + Clinical ... Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of...trial protocol development and reviews ( clinical trial protocols and medical device protocols) + ICF reviews… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …respect to the safety risk assigned remains top of mind in the context of patient management in the clinical trial setting and in the real-world setting. + ... CSPV and other internal groups) and outside of Daiichi Sankyo (eg clinical trial sites, CROs, collaboration partners); Supports effective direct communication… more
- Northwell Health (Staten Island, NY)
- …+ Supply necessary medical documentation to begin or continue treatment. + Supply clinical trial documentation for non-conventional treatment. + To ... with Patient Accounts, entry of collection notes, patient maintenance, trial balance, follow-ups as needed. + * Interacts with...* Required to maintain effective communication with the immediate management and staff of their assigned clinical … more
- Sanofi Group (Morristown, NJ)
- …IND/CTA submission strategy to ensure preparation timelines meet the project timelines for clinical trial initiation. + May lead submission teams or regulatory ... Experience with acceleration pathways (Orphan Drug, Breakthrough Therapy ), pediatric and clinical trial regulations as well as novel methodologies for… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …Years and Counting!** Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address ... timelines and resource planning, work in tandem with Biostatistics and Data Management members to ensure best vendor performance, monitor analysis dataset and TLFs… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …If you are interacting with CROs in the management of ex-US/ex-EU CTAs towards clinical trial activations preferred + If you have a high attention to detail; ... area. We are a hands-on culture so responsibilities will include support to some clinical study activities. The candidate will also supply , lead and/or supervise… more
- Sanofi Group (Morristown, NJ)
- …submission strategy to ensure preparation timelines meet the project timelines for clinical trial initiation. + Contributes to content and reviews regulated ... commercial and Global Regulatory Team for assigned projects + Liaises with clinical , medical, commercial, supply functions, and other internal business… more